scholarly journals Hereditary Gelsolin Amyloidosis: A New Japanese Case with Cutis Laxa as a Diagnostic Clue

2011 ◽  
Vol 91 (2) ◽  
pp. 201-203 ◽  
Author(s):  
A Asahina ◽  
T Yokoyama ◽  
M Ueda ◽  
Y Ando ◽  
N Ohshima ◽  
...  
Keyword(s):  
Cutis Laxa ◽  
Japanese Case ◽  
Diagnostic Clue

A Japanese case of segmental Darier's disease caused by mosaicism for the ATP2A2 mutation

2003 ◽  
Vol 149 (1) ◽  
pp. 185-188 ◽  
Author(s):  
T. Wada ◽  
Y. Shirakata ◽  
H. Takahashi ◽  
S. Murakami ◽  
H. Iizuka ◽  
...  
Keyword(s):  
Japanese Case ◽  
Darier’S Disease ◽  
Darier's Disease

scholarly journals A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene

2018 ◽  
Vol 57 (20) ◽  
pp. 3011-3014 ◽  
Author(s):  
Yuka Ebihara ◽  
Hitoshi Mochizuki ◽  
Nobuyuki Ishii ◽  
Ikuko Mizuta ◽  
Kazutaka Shiomi ◽  
...  
Keyword(s):  
Rare Mutation ◽  
Japanese Case ◽  
I Gene
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